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01 2GRANULES

02 2ACTAVIS TOTOWA

03 1AJANTA PHARMA LTD

04 2AMNEAL PHARMS

05 1ANNORA PHARMA

06 1ASPIRO

07 2AUROBINDO PHARMA LTD

08 3BAXTER HLTHCARE CORP

09 1BE PHARMS

10 1DEXCEL

11 2DR REDDYS LABS LTD

12 1EPIC PHARMA LLC

13 1EUGIA PHARMA

14 1FRESENIUS KABI USA

15 1GLAND PHARMA LTD

16 1HANGZHOU ZHONGMEI

17 2HETERO LABS LTD V

18 1HIKMA

19 1INGENUS PHARMS LLC

20 2JUBILANT GENERICS

21 1KNACK

22 1L PERRIGO CO

23 2LANNETT CO INC

24 2MACLEODS PHARMS LTD

25 2MANKIND PHARMA

26 1MEITHEAL

27 2MYLAN PHARMS INC

28 1NORVIUM BIOSCIENCE

29 2ORBION PHARMS

30 2RUBICON

31 1SANDOZ

32 4SUN PHARM

33 2SUN PHARM INDS LTD

34 2TEVA

35 1TEVA PARENTERAL

36 2TORRENT PHARMS

37 2WOCKHARDT BIO AG

38 4WYETH PHARMS

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PharmaCompass

01

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Pharma, Lab & Chemical Expo
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothGranules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

RLD : No

TE Code : AB

PANTOPRAZOLE SODIUM

Brand Name : PANTOPRAZOLE SODIUM

Dosage Form : TABLET, DELAYED RELEASE;ORAL

Dosage Strength : EQ 20MG BASE

Approval Date : 2023-12-11

Application Number : 217282

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Granules India

02

arrow
Pharma, Lab & Chemical Expo
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothGranules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

RLD : No

TE Code : AB

PANTOPRAZOLE SODIUM

Brand Name : PANTOPRAZOLE SODIUM

Dosage Form : TABLET, DELAYED RELEASE;ORAL

Dosage Strength : EQ 40MG BASE

Approval Date : 2023-12-11

Application Number : 217282

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Granules India

03

Pharma, Lab & Chemical Expo
Not Confirmed
arrow
arrow
Pharma, Lab & Chemical Expo
Not Confirmed

PANTOPRAZOLE SODIUM

Brand Name : PANTOPRAZOLE SODIUM

Dosage Form : TABLET, DELAYED RELEASE;ORAL

Dosage Strength : EQ 20MG BASE

Approval Date : 2007-09-10

Application Number : 77058

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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04

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

PANTOPRAZOLE SODIUM

Brand Name : PANTOPRAZOLE SODIUM

Dosage Form : INJECTABLE; INJECTION

Dosage Strength : 40MG

Approval Date :

Application Number : 22226

RX/OTC/DISCN :

RLD :

TE Code :

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05

Pharma, Lab & Chemical Expo
Not Confirmed
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arrow
Pharma, Lab & Chemical Expo
Not Confirmed

PANTOPRAZOLE SODIUM

Brand Name : PANTOPRAZOLE SODIUM

Dosage Form : TABLET, DELAYED RELEASE;ORAL

Dosage Strength : EQ 20MG BASE

Approval Date : 2007-08-02

Application Number : 77056

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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06

Pharma, Lab & Chemical Expo
Not Confirmed
arrow
arrow
Pharma, Lab & Chemical Expo
Not Confirmed

PANTOPRAZOLE SODIUM

Brand Name : PANTOPRAZOLE SODIUM

Dosage Form : TABLET, DELAYED RELEASE;ORAL

Dosage Strength : EQ 40MG BASE

Approval Date : 2007-08-02

Application Number : 77056

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

07

Pharma, Lab & Chemical Expo
Not Confirmed
arrow
arrow
Pharma, Lab & Chemical Expo
Not Confirmed

PANTOPRAZOLE SODIUM

Brand Name : PROTONIX

Dosage Form : TABLET, DELAYED RELEASE;ORAL

Dosage Strength : EQ 40MG BASE

Approval Date : 2000-02-02

Application Number : 20987

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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08

Pharma, Lab & Chemical Expo
Not Confirmed
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arrow
Pharma, Lab & Chemical Expo
Not Confirmed

PANTOPRAZOLE SODIUM

Brand Name : PROTONIX

Dosage Form : TABLET, DELAYED RELEASE;ORAL

Dosage Strength : EQ 20MG BASE

Approval Date : 2001-06-12

Application Number : 20987

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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09

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

PANTOPRAZOLE SODIUM

Brand Name : PROTONIX IV

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 40MG BASE/VIAL

Approval Date : 2001-03-22

Application Number : 20988

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AP

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10

Pharma, Lab & Chemical Expo
Not Confirmed
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arrow
Pharma, Lab & Chemical Expo
Not Confirmed

PANTOPRAZOLE SODIUM

Brand Name : PROTONIX

Dosage Form : FOR SUSPENSION, DELAYED RELEASE;ORAL

Dosage Strength : EQ 40MG BASE

Approval Date : 2007-11-14

Application Number : 22020

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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